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DuraDiagnost F30

EUDAMED

Class IIb (EU MDR)

Ref 712202

by Philips Healthcare (Suzhou) Co., Ltd.

Identity

Trade Name
DuraDiagnost F30 EUDAMED
Device Name
DuraDiagnost F30 EUDAMED
Model / Reference
712202 EUDAMED

Identifiers

Primary DI / UDI-DI
00884838095212 EUDAMED
Basic UDI-DI
0884838BM1057M6 EUDAMED
Direct Marketing DI
00884838095212 EUDAMED
EMDN Code
Z11031101 MULTIFUNCTIONAL SYSTEMS FOR DIRECT DIGITAL RADIOLOGY EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Stationary basic diagnostic x-ray system, digital

DuraDiagnost F30 by Philips Healthcare (Suzhou) Co., Ltd. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Stationary basic diagnostic x-ray system, digital.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000003923
Authorised Representative
Philips Medical Systems Nederland B.V. NL-AR-000001422

Sources (1)

  • EUDAMED 61133c51-5f4d-4563-8390-1b80a8edb778 61 fields · synced Jun 18, 2026